CNR Institutional Research Information System

LIGUORI, MARIA
 Distribuzione geografica
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Continente #
AS - Asia 3.922
NA - Nord America 1.564
EU - Europa 802
SA - Sud America 606
AF - Africa 66
OC - Oceania 8
Totale 6.968
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Nazione #
SG - Singapore 1.517
US - Stati Uniti d'America 1.500
CN - Cina 1.003
BR - Brasile 516
HK - Hong Kong 401
VN - Vietnam 369
IT - Italia 248
FR - Francia 224
KR - Corea 192
JP - Giappone 183
NL - Olanda 111
IN - India 65
AR - Argentina 41
DE - Germania 37
FI - Finlandia 34
GB - Regno Unito 34
BD - Bangladesh 33
IL - Israele 29
CA - Canada 26
ID - Indonesia 24
IQ - Iraq 21
EC - Ecuador 20
ZA - Sudafrica 20
ES - Italia 14
SE - Svezia 13
MA - Marocco 12
MX - Messico 12
TR - Turchia 12
AT - Austria 11
PL - Polonia 10
TN - Tunisia 10
UA - Ucraina 10
KE - Kenya 9
UZ - Uzbekistan 9
CL - Cile 8
IE - Irlanda 8
PH - Filippine 8
AU - Australia 7
CO - Colombia 7
RU - Federazione Russa 7
SA - Arabia Saudita 7
PK - Pakistan 6
AE - Emirati Arabi Uniti 5
MY - Malesia 5
PE - Perù 5
AZ - Azerbaigian 4
DO - Repubblica Dominicana 4
DZ - Algeria 4
JM - Giamaica 4
KG - Kirghizistan 4
KZ - Kazakistan 4
PT - Portogallo 4
SK - Slovacchia (Repubblica Slovacca) 4
TH - Thailandia 4
VE - Venezuela 4
BB - Barbados 3
CR - Costa Rica 3
GR - Grecia 3
NP - Nepal 3
PY - Paraguay 3
AL - Albania 2
BA - Bosnia-Erzegovina 2
BO - Bolivia 2
BZ - Belize 2
CZ - Repubblica Ceca 2
DK - Danimarca 2
EE - Estonia 2
HN - Honduras 2
HU - Ungheria 2
IR - Iran 2
JO - Giordania 2
LT - Lituania 2
MD - Moldavia 2
MT - Malta 2
SY - Repubblica araba siriana 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
BE - Belgio 1
BF - Burkina Faso 1
BG - Bulgaria 1
BS - Bahamas 1
BY - Bielorussia 1
CG - Congo 1
CH - Svizzera 1
CI - Costa d'Avorio 1
EG - Egitto 1
HR - Croazia 1
IM - Isola di Man 1
KW - Kuwait 1
LB - Libano 1
LK - Sri Lanka 1
LU - Lussemburgo 1
LV - Lettonia 1
MK - Macedonia 1
MM - Myanmar 1
MU - Mauritius 1
NG - Nigeria 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
OM - Oman 1
Totale 6.955
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Città #
Singapore 897
Santa Clara 582
Hefei 510
Hong Kong 396
San Jose 220
Seoul 191
Lauterbourg 173
Tokyo 151
Beijing 148
Ho Chi Minh City 145
Dallas 90
Ashburn 86
Hanoi 76
Los Angeles 70
São Paulo 41
Rome 34
New York 30
Buffalo 28
Minamishinagawa 28
Helsinki 26
Bengaluru 18
Da Nang 18
Milan 18
Rio de Janeiro 16
Haiphong 14
Frankfurt am Main 13
Belo Horizonte 11
Brasília 11
Porto Alegre 11
Amsterdam 10
Bari 10
Dhaka 10
Guarulhos 10
Campinas 9
Cape Town 9
Curitiba 9
Orem 9
Tashkent 9
Toronto 9
Barcellona Pozzo di Gotto 8
Fortaleza 8
Ha Long 8
Nairobi 8
Nuremberg 8
Surabaya 8
Thái Bình 8
Anoia Superiore 7
Baghdad 7
Biên Hòa 7
Brooklyn 7
Chicago 7
Dublin 7
Florence 7
Guangzhou 7
Turin 7
Warsaw 7
Bologna 6
Buenos Aires 6
Cabo Frio 6
Can Tho 6
Guayaquil 6
Johannesburg 6
London 6
Manaus 6
Naples 6
Potenza 6
Quito 6
Quận Bình Thạnh 6
Salvador 6
Santo André 6
Stockholm 6
Sydney 6
Tunis 6
Boston 5
Chennai 5
Lappeenranta 5
Manchester 5
Montreal 5
New Delhi 5
Portsmouth 5
Shanghai 5
São Bernardo do Campo 5
São José do Rio Preto 5
Vienna 5
Washington 5
Assago 4
Baku 4
Bauru 4
Bishkek 4
Casablanca 4
Catania 4
Caxias do Sul 4
Delhi 4
Düsseldorf 4
Goiânia 4
Hải Dương 4
Joinville 4
Las Vegas 4
Lima 4
Medford 4
Totale 4.494
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Nome #
Tay Sachs in South Italy 148
An early Transcriptomic Investigation in Adult Patients with Spinal Muscular Atrophy Under Treatment with Nusinersen 107
Sex and Gender Differences in Neurodegenerative Diseases: Challenges for Therapeutic Opportunities 93
A Pilot Longitudinal Evaluation of MicroRNAs for Monitoring the Cognitive Impairment in Pediatric Multiple Sclerosis 92
MicroRNA and transcription factor co-regulatory network analysis: a combined bioinformatics and molecular strategy for uncovering genetic hub regulatory elements in multiple sclerosis pathogenesis 87
Medicina di Precisione in Pediatria - Biotecnologie e applicazioni per lo sviluppo e la salute 85
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis 84
Associazione tra la subunità 2B del recettore NMDA (gene GRIN2B) e la malattia di Alzheimer 83
Impact of individual cognitive profile on visuo-motor reorganization in relapsing-remitting multiple sclerosis 82
Investigating the Role of MicroRNA and Transcription Factor Co-regulatory Networks in Multiple Sclerosis Pathogenesis 80
Counting of peripheral extracellular vesicles in Multiple Sclerosis patients by an improved nanoplasmonic assay and dynamic light scattering 80
NOS2A AS CANDIDATE GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS: AN HAPLOTYPE STUDY BY USING A SUBSETS OF SNPs. 78
Mutational screening of the eIF2B5 gene in sib pairs affected by multiple sclerosis. 77
Conventional MRI and NOTCH3 gene screening in sporadic CADASIL. 76
Functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis 73
Treating epilepsy in Italy between XIX and XX century 73
Neuropsychological impact on motor reorganization in relapsing remitting multiple sclerosis 72
Two Novel Cysteine-Sparing Notch3 Mutations In Patients With CADASIL 67
Glutamate and multiple sclerosis. 64
A novel missense mutation (p.Arg309His) in the nuclear localization signal sequence of spastin protein causes a complicated form of Hereditary Spastic Paraplegia 63
Fukutin-Related Protein L276I mutation in Limb Girdle Muscular Dystrophy patients with a Duchenne/Becker like phenotype 63
The effects of BDNF Val(66)Met polymorphism on brain function in controls and patients with multiple sclerosis: An imaging genetic study. 62
Investigation of the relationship between anti-GM1 antibodies and brain atrophy in multiple sclerosis 62
Apolipoprotein E genotype does not influence the progression of multiple sclerosis. 59
Association between miRNAs expression and cognitive performances of Pediatric Multiple Sclerosis patients: A pilot study 59
First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegia. 58
A novel mutation (Thr116Ile) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease. 57
Changes of serum sICAM-1 and MMP-9 induced by rIFNbeta-1b treatment in relapsing-remitting MS 57
Meta-Analysis of Differential Connectivity in Gene Co-Expression Networks in Multiple Sclerosis 56
CAV3 T78M MUTATION IN HETEROZYGOSIS IS NOT ASSOCIATED WITH LGMD1C IN SOUTHERN ITALY 55
Investigating the Role of MicroRNA and Transcription Factor Co-regulatory Networks in Multiple Sclerosis Pathogenesis 53
Molecular signatures associated with cognitive dysfunctions in pediatric multiple sclerosis 53
A Predictive Model for MicroRNA Expressions in Pediatric Multiple Sclerosis Detection 52
Molecular Characterization of Peripheral Extracellular Vesicles in Clinically Isolated Syndrome: Preliminary Suggestions from a Pilot Study. 52
Gene symbol: NOTCH3 51
A family with dominant optic atrophy and deafness due to a novel Opa1 mutation. 50
An Investigation of the Role of Common and Rare Variants in a Large Italian Multiplex Family of Multiple Sclerosis Patients 49
Dysregulation of MicroRNAs and Target Genes Networks in Peripheral Blood of Patients With Sporadic Amyotrophic Lateral Sclerosis 49
Combined microRNA and mRNA expression analysis in pediatric multiple sclerosis: an integrated approach to uncover novel pathogenic mechanisms of the disease. 49
A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy 48
CSF MALDI-TOF mass spectrometry protein profiling in Clinically Isolated Syndrome. 48
Identification of a patient affected by "Juvenile-chronic" Tay Sachs disease in South Italy. 48
Axonal damage in multiple sclerosis plaques: a combined magnetic resonance imaging and 1H-magnetic resonance spectroscopy study 47
Age at onset in multiple sclerosis 46
Cognitive impairment and brain atrophy in patients with relapsing-remitting Multiple Sclerosis (RRMS): the role of brain derived neurotrophic factor (BDNF) gene. 46
Peripheral mRNA expression of brain-derived neurotrophic factor Val66Met polymorphism in patients with relapsing-remitting multiple sclerosis 45
Fas antigen and sporadic Alzheimer's disease in Southern Italy:evaluation of two polymorphisms in the TNFRSF6 gene. 43
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 43
The influence of age at onset on the course of multiple sclerosis 43
COGNITIVE DYSFUNCTION AND QUALITY OF LIFE IN MULTIPLE SCLEROSIS DISEASE 42
Gly269Ser mutation in compound heterozygosity with Leu127Arg is associated with adult onset of Tay-Sachs: a case report from south Italy 41
Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis 41
Listening to the neurological teams for multiple sclerosis: the SMART project 41
ADULT ONSET TAY-SACHS ASSOCIATED WITH -HEXOSAMINIDASE A DEFICIENCY: A CASE REPORT FROM SOUTH ITALY 40
Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease 40
Ventro-Lateral Prefrontal activity during working-memory processing is modulated by Monoamine oxidase-A genetic variation 40
Mutation analysis of the GRIN2B gene in Alzheimer's disease 40
Brain-Derived Neurotrophic Factor Val66Met polymorphism and peripheral mrna expression in patients with Relapsing Remitting Multiple Sclerosis (RRMS). 40
Impact of individual cognitive profile on visuo-motor reorganization in relapsing-remitting multiple sclerosis 40
Proteomic profiling in multiple sclerosis clinical courses reveals potential biomarkers of neurodegeneration 40
Visualizing genetic influences on Human brain function: Interactive effects of BNDF and COMT allelic variations on a spatial working memory network 39
Course and prognosis in early-onset MS: comparison with adult-onset forms. 38
D678N mutation in a patient with an early-onset Alzheimer's Disease 38
Neuropatia ottica ereditaria di Leber s e Sclerosi Multipla: Harding s syndrome. 38
Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia 38
Neurobiological mechanisms underlying emotional processing in Relapsing-Remitting Multiple Sclerosis 38
Polymorphisms and mutational analysis of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy. 37
Assenza di correlazione tra sclerosi multipla familiare (SM) e mutazioni nel gene eIF2B5. 37
APP gene mutation (D678N) in a patient with an Early-Onset Alzheimer's Disease 37
Familial Alzheimer's disease with amyloid precursor protein D678N mutation: a case report 37
The role of mri in the NOTCH3 gene screening of apparently sporadic CADASIL 36
A phenotyphic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation. 36
Impact of brain atrophy and cognitive profile on visuo-motor reorganization in relapsing-remitting multiple sclerosis 36
PROGRESSION OF MOBILITY IMPAIRMENT AND BRAIN WHITE MATTER LESION VOLUME IN THE ELDERLY: A TWO-YEAR LONGITUDINAL STUDY 35
Preliminary evidences of a NOS2A protective effect from Relapsing-Remitting Multiple Sclerosis 35
PERIPHERAL MRNA EXPRESSION OF BRAIN-DERIVED NEUROTROPHIC FACTOR VAL66MET POLYMORPHISM IN PATIENTS WITH RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS). 35
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes 35
Neuropsychological influence on motor reorganization in relapsing remitting MS patients 35
Brain-derived Neurotrophic Factor Val66Met polimorphism and the cortical response to spatial working memory. 34
Anti-GM1 antibodies are not associated with cerebral atrophy in patients with multiple sclerosis. 34
Neurofunctional correlates of personality traits in relapsing-remitting multiple sclerosis: an fMRI study. 34
Brain-derived neurotrophic factor and risk for primary adult-onset cranial-cervical dystonia 33
BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF) GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS): LONGITUDINAL EVALUATION 33
Serum prolactin concentrations in patients with multiple sclerosis 33
CADASIL: extended polymorphisms and mutational analysis of the NOTCH3 gene. 32
Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis 32
Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification 32
Trauma cranico e genotipo APO-E: causa o rischio di malatia di Alzheimer? 32
DISTINGUISHING APPARENTLY SPORADIC CADASIL FROM OTHER LEUCOENCEPHALOPATHIES:THE ROLE OF MAGNETIC RESONANCE IMAGING IN THE NOTCH3 GENE SCREENING 31
An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population 31
Depression and Parkinson's disease:a neuropsychological view 31
Screening for MELAS mutations in Italian patients having stroke-like episodes. 31
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy 31
CADASIL: molecular screening of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy. 31
CA repeat estrogen receptor b gene polymorphism in patients with Multiple Sclerosis. 31
Preliminary evidences of a NOS2A protective effect from relapsing-remitting multiple sclerosis. 30
Genetic screening of Alzheimer's disease genes in Italian samples yields novel mutations in Presenilin-enhancer 2. 30
High resolution proton MR spectroscopy of cerebrospinal fluid in MS patients. Comparison with biochemical changes in demyelinating plaques 30
Brain-derived neurotrophic factor val66met polymorphysm and the cortical response to spatial working memory 30
Ventro-Lateral Prefrontal activity during working memory processing is modulated by MAO A genetic variation. 30
Totale 4.968
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Categoria #
all - tutte 22.357
article - articoli 13.285
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 174
Totale 35.816
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202472 0 0 0 0 0 0 0 0 49 0 18 5
2024/20252.697 7 17 185 105 655 51 37 84 57 165 699 635
2025/20264.353 273 513 494 636 702 197 633 230 335 241 99 0
Totale 7.122